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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0001613,
umls-concept:C0001629,
umls-concept:C0007589,
umls-concept:C0007776,
umls-concept:C0020987,
umls-concept:C0022655,
umls-concept:C0025148,
umls-concept:C0039195,
umls-concept:C0205160,
umls-concept:C0814999,
umls-concept:C0949399,
umls-concept:C1511938,
umls-concept:C1550278,
umls-concept:C1709634
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pubmed:issue |
6
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pubmed:dateCreated |
1981-1-29
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pubmed:abstractText |
To analyze the developmental and functional interrelationship between cortical and medullary thymocytes, the peanut agglutinin-(PNA) binding capacity was used to separate thymocytes into PNA+ (cortical) and PNA- (medullary) thymocytes. Virtually, all positively selected PNA+ thymocytes (90% of the overall thymocyte population) expressed the Lyt 123 phenotype, whereas 90% of negatively selected PNA- thymocytes expressed Lyt 1 alloantigens, about 10% being Lyt 123 thymocytes. Provided, the requirement of Lyt 1 T helper cells was bypassed by Interleukin 2, a nonspecific mediator of T help, PNA+ Lyt 123 thymocytes mounted cytotoxic T cell responses comparable in magnitude to that of peripheral T cells. Their repertoire included antigenic disparities coded for by the complete MHC complex, H-2K, I-A, H-2D, mutational events at H-2K, as well as antigenic disparities expressed on TNP conjugated- and Sendai virus-infected syngeneic cells. PNA- Lyt 123 thymocytes represent a highly reactive pool of primary cytotoxic T lymphocyte (CTL) precursors for both alloreactive and H-2-restricted CTL responses. Since PNA- thymocytes include also Lyt 1 T helper cells, PNA- responder thymocytes are able to mount autonomously (CTL responses. Our data are first to provide direct evidence that Lyt 123 cells represent a common source of alloreactive and H-2-restricted CTL precursors in unprimed lymphocyte populations. Moreover, the apparent immunocompetence of cortical PNA+ thymocytes is now explained by their lack of T helper cells.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
125
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2532-8
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:6159411-Agglutinins,
pubmed-meshheading:6159411-Animals,
pubmed-meshheading:6159411-Arachis hypogaea,
pubmed-meshheading:6159411-Cell Differentiation,
pubmed-meshheading:6159411-Cell Separation,
pubmed-meshheading:6159411-Chromatography, Affinity,
pubmed-meshheading:6159411-Cytotoxicity, Immunologic,
pubmed-meshheading:6159411-Epitopes,
pubmed-meshheading:6159411-Isoantigens,
pubmed-meshheading:6159411-Mice,
pubmed-meshheading:6159411-Mice, Inbred BALB C,
pubmed-meshheading:6159411-Mice, Inbred C57BL,
pubmed-meshheading:6159411-Mice, Inbred CBA,
pubmed-meshheading:6159411-Phenotype,
pubmed-meshheading:6159411-T-Lymphocytes,
pubmed-meshheading:6159411-Thymus Gland
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pubmed:year |
1980
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pubmed:articleTitle |
Intrathymic differentiation of cytotoxic T lymphocyte (CTL) precursors. I. The CTL immunocompetence of peanut agglutinin-positive (cortical) and negative (medullary) Lyt 123 thymocytes.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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